Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tseng, Chih-Chung | en_US |
dc.contributor.author | Tasi, Cheng-Hsun | en_US |
dc.contributor.author | Sun, Chung-Ming | en_US |
dc.date.accessioned | 2014-12-08T15:23:13Z | - |
dc.date.available | 2014-12-08T15:23:13Z | - |
dc.date.issued | 2012-06-01 | en_US |
dc.identifier.issn | 1386-2073 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/16294 | - |
dc.description.abstract | A novel protocol for rapid assemble of benzimidazole framework has been demonstrated. This method incorporated with light fluorous-tag provides a convenient method for diversification of benzimidazoles and for easy purification via fluorous solid-phase extraction (F-SPE) in a parallel manner. The key transformation of this study involves in situ reduction of aromatic nitro compound, amide formation, cyclization and aromatization promoted by microwave irradiation in a one-pot fashion. The strategy is envisaged to be applied for the establishment of drug-like small molecule libraries for high throughput screening. | en_US |
dc.language.iso | en_US | en_US |
dc.subject | Benzimidazoles | en_US |
dc.subject | bioactive heterocycles | en_US |
dc.subject | fluorous synthesis | en_US |
dc.subject | F-SPE | en_US |
dc.subject | microwave chemistry | en_US |
dc.title | Light Fluorous-Tagged Traceless One-Pot Synthesis of Benzimidazoles Facilitated by Microwave Irradiation | en_US |
dc.type | Article | en_US |
dc.identifier.journal | COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING | en_US |
dc.citation.volume | 15 | en_US |
dc.citation.issue | 5 | en_US |
dc.citation.epage | 411 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000304043600006 | - |
dc.citation.woscount | 2 | - |
Appears in Collections: | Articles |